Issue 41, 2015

Palladium-catalyzed one-pot synthesis of diazoles via tert-butyl isocyanide insertion

Abstract

An efficient one-pot palladium-catalyzed reaction for the synthesis of diazoles from readily available hydrazides and aryl halide via isocyanide insertion/cyclization sequence has been developed. This methodology efficiently constructs diazoles in good to excellent yields with the advantages of wide functional group tolerance and operational simplicity.

Graphical abstract: Palladium-catalyzed one-pot synthesis of diazoles via tert-butyl isocyanide insertion

Supplementary files

Article information

Article type
Paper
Submitted
30 Jun 2015
Accepted
18 Aug 2015
First published
19 Aug 2015

Org. Biomol. Chem., 2015,13, 10402-10408

Palladium-catalyzed one-pot synthesis of diazoles via tert-butyl isocyanide insertion

X. Fan, X. Jiang, Y. Zhang, Z. Chen and Y. Zhu, Org. Biomol. Chem., 2015, 13, 10402 DOI: 10.1039/C5OB01328C

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